What is NDC 50844-714?

50844-714 is the product NDC for Naproxen Back and Muscle Pain (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by L.N.K. International, Inc.. It has 6 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Naproxen Back and Muscle Pain (Naproxen Sodium).

L.N.K. International, Inc., NDC labeler code 50844. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Naproxen Back and Muscle Pain?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Naproxen Back and Muscle Pain NDC 50844-714

NDC codes

FDA NDC Directory

Product NDC (as listed)50844-714Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50844-0714Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
50844-714-14	5084407141450844071414	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)Marketed from Feb 1, 2019
50844-714-16	5084407141650844071416	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)Marketed from Feb 1, 2019
50844-714-19	5084407141950844071419	1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Feb 1, 2019
50844-714-56	5084407145650844071456	25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)Marketed from Feb 1, 2019
50844-714-98	5084407149850844071498	8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)Marketed from Feb 1, 2019
50844-714-99	5084407149950844071499	8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)Marketed from Feb 1, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Naproxen Back and Muscle Pain
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: L.N.K. International, Inc.NDC labeler code 50844
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204872
Marketing start: Feb 1, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8abSPL ID bc397444-6e0e-4b4e-8f03-d6372588d8abSPL set ID 68944663-0dc0-4d3a-a36b-019061bdbfa0RxCUI 849574UNII 9TN87S3A3CUPC 0350844714169
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450844071414 followed by a unit qualifier and the quantity

Package 50844-0714-14. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 9, 2026.

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains due to: backache muscular aches minor pain of arthritis toothache the common cold menstrual cramps headache temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50844-714

What is NDC 50844-714?: 50844-714 is the product NDC for Naproxen Back and Muscle Pain (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by L.N.K. International, Inc.. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen Back and Muscle Pain (Naproxen Sodium).
What is the active ingredient?: Naproxen sodium.
Who is the labeler?: L.N.K. International, Inc., NDC labeler code 50844. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Naproxen Back and Muscle Pain?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 204872

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 204872
Product	Strength	Form · route	Labeler	Product NDC
24/7 Life by 7-Eleven Naproxen Sodiumnaproxen sodium tablet, film coated	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Lil' Drug Store Products, Inc.	66715-5428
All Day Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	WALMART INC.	79903-005
AnaDentnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Belmora LLC	27854-170
Artridolnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Zapotol Products Corp	59428-604
Back and Muscle Painnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Rite Aid Corporation	11822-4170
Back and Muscle Painnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	51316-817
First Aid Direct All Day Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Cintas Corporation	42961-122
Flanaxnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Belmora LLC	27854-160
Flanax Menstrual Pain Relievernaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Belmora LLC	27854-165
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Better Living Brands, LLC	21130-674
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Amerisource Bergen	46122-562
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Amerisource Bergen	46122-564
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	L.N.K. International, Inc.	50844-261
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Family Dollar Services Inc	55319-406
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Family Dollar Services Inc	55319-717
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	Geri-Care Pharmaceutical Corp	57896-954
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5039
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7572
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	Proficient Rx LP	71205-595
Naproxennaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	Bryant Ranch Prepack	71335-1282

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Naproxen Back and Muscle Pain (Naproxen sodium) NDC 50844-714